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engineered a peptide derived from the amino acid sequence surrounding the C272 site of PD-L1, which competitively inhibited the palmitoylation of endogenous PD-L1 by ZDHHC3, thereby diminishing PD-L1 expression in tumour cells and enhancing T-cell-mediated antitumour immunity [55]

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doi:10.1002/ptr.6848

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